past events
- 2011-
program
- Bayesian Goldilocks Designs: Getting the Sample Size Just Right, Scott M. Berry
- Adapting Traditional Adaptive Designs: New Methods and Procedures, Scott Evans
- Efficient Two-Stage Adaptive Designs with Sample Size Adjustment, Qing Liu et. al
- Bayesian and Frequentist Adaptive Designs in Clinical Trials, Gene Pennello
-
2008
- Case Studies of the Use of Meta-Analyses of Drug Safety Questions in the Regulatory Setting, Jesse A. Berlin
- Role of Integrated Analysis in Regulatory Applications, H.M. James Hung
- Integrated Dose-Exposure-Response Modeling and Use in Clinical Trial Simulation, Heinz Schmidli and Jerry R. Nedelman
- Meta-analysis in randomized clinical trials with low event rates, Jonathan J. Shuster
- 2007-
program
- Global Sensitivity Analysis for Randomized Trials with Competing Causes of Drop-out, Daniel O. Scharfstein
- Non-inferiority Methodology in Drug Clinical Trial, H.M. James Hung
- Sensitivity to MAR Assumption in Missing Data: Case Studies Using Model-Based Multiple Imputation, Jie Zhang and José Pinheiro
- Parametric Modeling of Time-to-Event Data With Possibly Non-Proportional Hazards, Keaven Anderson